{
    "disease_id": "DOID:0070675",
    "recommended_name": {
        "id": "DOID:0070675",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070675",
        "name": "autosomal recessive nonsyndromic deafness 121",
        "description": "An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual moderate sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the GPR156 gene on chromosome 3q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070675",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070675",
            "name": "DFNB121",
            "description": ""
        },
        {
            "id": "MONDO:0957825",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957825",
            "name": "hearing loss, autosomal recessive 121",
            "description": ""
        },
        {
            "id": "MONDO:0957825",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957825",
            "name": "deafness, autosomal recessive 121",
            "description": ""
        },
        {
            "id": "MIM:620551",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620551",
            "name": "Deafness, autosomal recessive, 121",
            "description": "Deafness, autosomal recessive, 121"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070675"
    ],
    "unlinked_id_list": []
}